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Clinical Trial Associate

AL Solutions
england, united kingdom, united kingdom
1 month ago
Applications closed

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Taylor Young is looking for a Clinical Trial Associate in the UK for a Global CRO


Join a leading global Contract Research Organization (CRO) dedicated to providing high-quality clinical research services to pharmaceutical, biotechnology, and medical device companies. With a global presence and a commitment to innovation, we drive efficiency and excellence across all phases of clinical development.


As a Clinical Trial Associate (CTA), you will support the clinical operations team in the planning, execution, and tracking of clinical trials across multiple therapeutic areas and global sites. You will be instrumental in maintaining trial documentation, coordinating project communications, and ensuring compliance with regulatory and company standards.


Key Responsibilities:


  • Assist in the preparation, collection, and maintenance of essential clinical trial documents (eTMF/TMF).
  • Support study start-up, conduct, and close-out activities in collaboration with Clinical Research Associates (CRAs), Project Managers (PMs), and regulatory teams.
  • Track site submissions, approvals, and overall study timelines and milestones.
  • Coordinate meetings, teleconferences, and documentation (e.g., agenda preparation, meeting minutes).
  • Ensure compliance with ICH-GCP, SOPs, and applicable regulatory guidelines.
  • Assist with budget tracking, vendor management, and investigator payments as needed.
  • Support audit readiness by maintaining accurate and timely documentation.
  • Communicate effectively with internal and external stakeholders including study sites, vendors, and sponsors.


Qualifications:


  • Bachelor’s degree in Life Sciences, Healthcare, or a related field.
  • 1–2 years of experience in a clinical research environment (ideally within a CRO).
  • Strong understanding of clinical trial processes, ICH-GCP, and regulatory requirements.
  • Proficiency in MS Office Suite (Word, Excel, Outlook) and clinical trial management systems (e.g., eTMF, CTMS).
  • Excellent organizational skills with attention to detail and the ability to manage multiple priorities.
  • Strong written and verbal communication skills.
  • Ability to work independently and as part of a collaborative, cross-functional team.


Please apply if you are wanting more details!

National AI Awards 2025

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